Insights / Life Sciences
Which parts of a medical device label and IFU must be in Arabic for the Saudi market, what the SFDA texts say, and a checklist to prepare your file.
Quick Answer
SFDA Arabic labeling rules require Arabic and English information for medical devices used by lay persons and for self-testing IVDs. That covers the instructions for use, the electronic user interface, the Arabic rendering of the device name and promotional material. Devices for healthcare professionals must be understood by their users, and SFDA can request service documents in Arabic.
SFDA Arabic labeling requires that information supplied with devices for lay persons be in both Arabic and English. The main source is the SFDA document Requirements for Medical Devices Marketing Authorization (MDS-REQ 1), version 6.0, dated December 19, 2021. Its Annex 1 sets the Essential Principles that a Medical Device Marketing Authorization (MDMA) file must meet.
For devices other than IVDs:
For self-testing IVDs, the information supplied, the electronic interface and the Arabic device name follow the same bilingual rule (Essential Principles 19.1, 20.1(a) and 20.2(a)).
The Arabic requirement in MDS-REQ 1 targets lay users, so audience decides most of the answer. For professional-use devices, IFUs must be “written in terms readily understood by the intended user,” and the bilingual rule is not repeated. Three rules reach beyond the label:
Trade guidance points the same way. The US Commercial Service Saudi Arabia labeling and marking page (May 2026) states that warnings and safety instructions must be in Arabic, or Arabic and English, and that instruction manuals must be in Arabic or both languages. It refers device exporters to the SFDA Medical Device Department for full rules.
Device-specific guidances can name exactly which items need Arabic. A clear example is MDS-G-014, Guidance on Content of Labeling of Contact Lenses and its Solutions, version 3.0, dated October 1, 2024.
It requires labeling written in English. When the product is intended for a lay person, it also requires Arabic for:
The product name must also appear in English and in Arabic “as it is pronounced in English.” And the translated labeling must be approved by the manufacturer and kept in the technical documentation. That makes the manufacturer accountable for the Arabic text, so you need a review step and a record of it.
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Yes, MDS-REQ 1 allows electronic IFUs that meet Annex 10, which requires:
For IVDs, eIFU is limited to professional-use devices and excludes near-patient testing (Essential Principle 20.1(f)). Labeling must not include the SFDA logo, though it may show the Medical Device National Listing Number (Essential Principle 23.1(i)).
Use this table to check your file before submission.
| Item | Arabic needed? | Source |
|---|---|---|
| Information supplied with lay-person devices (label and IFU) | Yes, Arabic and English | MDS-REQ 1, EP 23.1(a) |
| Electronic user interface, lay-person devices | Yes, Arabic and English | MDS-REQ 1, EP 22.1 |
| Device name on label, lay-person devices | Arabic name as pronounced in English | MDS-REQ 1, EP 23.2(a) |
| Self-testing IVD information and interface | Yes, Arabic and English | MDS-REQ 1, EP 19.1, 20.1(a) |
| Promotional material, lay-person devices | Yes, Arabic and English | MDS-REQ 1, Annex 3 |
| Service, storage and disposal instructions | English; Arabic on request | MDS-REQ 1, Annex 3 |
| Implant patient information | Yes, Arabic and English | MDS-REQ 1, Annex 8 |
| Contact lens IFU and labels, lay use | Yes, as listed in the guidance | MDS-G-014 v3.0 |
| Manufacturer approval of translated labeling | Required, kept in technical file | MDS-G-014 v3.0 |
| Saudi-market eIFU | Must be clearly identified | MDS-REQ 1, Annex 10 |
Start from a locked English source, then translate, review and file the Arabic as a controlled document. A practical sequence:
Requirements change, so confirm current SFDA labeling rules with the SFDA or qualified regulatory counsel before you submit. This article is informational only and is not regulatory advice.
Other Gulf markets also expect Arabic on labels, though device rules come from each health regulator. US Commercial Service guides state general labeling rules:
These pages cover goods broadly, so check each health regulator’s device rules before reusing a Saudi IFU.
Not under MDS-REQ 1 alone. The bilingual rule applies to lay-person devices and self-testing IVDs. Professional-use IFUs must be readily understood by the intended user, and service documents must be available in Arabic on request.
SFDA asks for the device name in Arabic “as it is pronounced in English,” in both MDS-REQ 1 and MDS-G-014. That is the trade name written in Arabic script so it sounds like the English name. Keep the same rendering on every label, IFU and screen.
MDS-REQ 1 allows eIFU when Annex 10 conditions are met, including a risk assessment and version control. The Saudi-market IFU must be clearly identified and open without an account or password.
The manufacturer. MDS-G-014 states that translated labeling must be approved by the manufacturer and kept in its technical documentation. Record who translated, reviewed and approved each version.
How Afrasia Trans Can Help
Afrasia Trans provides Arabic translation and multilingual DTP solutions for medical device labels, IFUs, eIFUs and software interfaces. Our linguists work by dialect and market, so written content follows Modern Standard Arabic while lay terminology is checked for Gulf readers. We can build your terminology list, translate and review label and IFU text, and lay out right-to-left artwork. See our life sciences and medical device solutions and the full list of languages we cover. Ready to prepare your SFDA file? Contact us for a quote.
About the Author
Mohamed Salah writes the Afrasia Trans industry guides on media, gaming, AI data, life sciences, legal and travel localization.
Sources
This article is for general information only. It is not legal, regulatory or medical advice.
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